PubMed for id: 333083

Year	Number of Results
1993	2
1999	1
2000	1
2004	2
2005	1
2007	1
2008	2
2009	2
2010	3
2011	1
2012	5
2013	1
2014	1
2015	2
2016	1
2017	2
2018	2
2019	6
2020	5
2021	79
2022	210
2023	186
2024	66

1

Gait Impairments in Patients Without Lower Limb Hypertonia Early Poststroke Are Related to Weakness of Paretic Knee Flexors.

Chow JW, Stokic DS. Chow JW, et al. Arch Phys Med Rehabil. 2019 Jun;100(6):1091-1101. doi: 10.1016/j.apmr.2018.10.014. Epub 2018 Nov 14. Arch Phys Med Rehabil. 2019. PMID: 30447195

2

Casting for upper limb hypertonia: a retrospective study to determine the factors associated with intervention decisions.

Kuipers K, Burger L, Copley J. Kuipers K, et al. NeuroRehabilitation. 2012;31(4):409-20. doi: 10.3233/NRE-2012-00811. NeuroRehabilitation. 2012. PMID: 23232165

3

Coactivation of ankle muscles during stance phase of gait in patients with lower limb hypertonia after acquired brain injury.

Chow JW, Yablon SA, Stokic DS. Chow JW, et al. Clin Neurophysiol. 2012 Aug;123(8):1599-605. doi: 10.1016/j.clinph.2012.01.006. Epub 2012 Feb 9. Clin Neurophysiol. 2012. PMID: 22325644

4

Long-term effect of shock wave therapy on upper limb hypertonia in patients affected by stroke.

Manganotti P, Amelio E. Manganotti P, et al. Stroke. 2005 Sep;36(9):1967-71. doi: 10.1161/01.STR.0000177880.06663.5c. Epub 2005 Aug 18. Stroke. 2005. PMID: 16109905 Clinical Trial.

5

Novel TARS2 variant identified in a Chinese patient with mitochondrial encephalomyopathy and a systematic review.

He P, Wang Q, Hong X, Yuan H. He P, et al. Am J Med Genet A. 2023 Jan;191(1):70-76. doi: 10.1002/ajmg.a.62988. Epub 2022 Oct 11. Am J Med Genet A. 2023. PMID: 36218002

6

A Rare Cause of Globus Pallidus and Dentate Nucleus Hyperintensity in Childhood: MBOAT Mutation.

Ozpinar E, Kaytan I, Topcu Y, Kılıc B, Aydin K. Ozpinar E, et al. Neurol India. 2021 Nov-Dec;69(6):1838-1840. doi: 10.4103/0028-3886.333478. Neurol India. 2021. PMID: 34979703 Free article.

7

Postmortem whole-genome sequencing on a dried blood spot identifies a novel homozygous SUOX variant causing isolated sulfite oxidase deficiency.

Owen MJ, Lenberg J, Feigenbaum A, Gold J, Chau K, Bezares-Orin Z, Ding Y, Chowdhury S, Kingsmore SF. Owen MJ, et al. Cold Spring Harb Mol Case Stud. 2021 Jun 11;7(3):a006091. doi: 10.1101/mcs.a006091. Print 2021 Jun. Cold Spring Harb Mol Case Stud. 2021. PMID: 34117075 Free PMC article.

8

A novel and recurrent KLHL40 pathogenic variants in a Chinese family of multiple affected neonates with nemaline myopathy 8.

Yi S, Zhang Y, Qin Z, Yi S, Zheng H, Luo J, Li Q, Wang J, Yang Q, Li M, Chen F, Zhang Q, Zhang Q, Shen Y. Yi S, et al. Mol Genet Genomic Med. 2021 Jun;9(6):e1683. doi: 10.1002/mgg3.1683. Epub 2021 May 12. Mol Genet Genomic Med. 2021. PMID: 33978323 Free PMC article.

9

A description of novel variants and review of phenotypic spectrum in UBA5-related early epileptic encephalopathy.

Briere LC, Walker MA, High FA, Cooper C, Rogers CA, Callahan CJ, Ishimura R, Ichimura Y, Caruso PA, Sharma N, Brokamp E, Koziura ME, Mohammad SS, Dale RC, Riley LG; Undiagnosed Diseases Network; Phillips JA, Komatsu M, Sweetser DA. Briere LC, et al. Cold Spring Harb Mol Case Stud. 2021 Jun 11;7(3):a005827. doi: 10.1101/mcs.a005827. Print 2021 Jun. Cold Spring Harb Mol Case Stud. 2021. PMID: 33811063 Free PMC article.

10

Novel compound heterozygous TARS2 variants in a Chinese family with mitochondrial encephalomyopathy: a case report.

Li X, Peng B, Hou C, Li J, Zeng Y, Wu W, Liao Y, Tian Y, Chen WX. Li X, et al. BMC Med Genet. 2020 Nov 5;21(1):217. doi: 10.1186/s12881-020-01149-0. BMC Med Genet. 2020. PMID: 33153448 Free PMC article.

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